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rs16921914

From SNPedia

Orientationplus
Stabilizedplus
Make rs16921914(A;A)
Make rs16921914(A;G)
Make rs16921914(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position31189224
GeneLOC100508736
is asnp
is mentioned by
dbSNPrs16921914
ebirs16921914
HLIrs16921914
Exacrs16921914
Varsomers16921914
Maprs16921914
PheGenIrs16921914
hapmaprs16921914
1000 genomesrs16921914
hgdprs16921914
ensemblrs16921914
gopubmedrs16921914
geneviewrs16921914
scholarrs16921914
googlers16921914
pharmgkbrs16921914
gwascentralrs16921914
openSNPrs16921914
23andMers16921914
23andMe allrs16921914
SNP Nexus

SNPshotrs16921914
SNPdbers16921914
MSV3drs16921914
GWAS Ctlgrs16921914
GMAF0.2309
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19801982OA-icon.png]
Trait Bone mineral density (spine)
Title Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Risk Allele A
P-val 2E-9
Odds Ratio 0.08 [0.05-0.11] sd increase


[PMID 19172991OA-icon.png] Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).


GET Evidence
rs16921914
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.25
summary